On-chip Parallel Detection of Shiga Toxin Producing Escherichia Coli Using Loop-mediated Isothermal Amplification
نویسندگان
چکیده
Shiga toxin-producing Escheria coli (STEC) strains are virulent agents responsible for thousands of illnesses in the United States [1]. The most common and notorious STEC serotype is O157:H7 but other serotypes, like O104:H4 responsible for May 2011 HUS outbreak in Germany [2], are responsible for one third of STEC related illness. Beginning on June of 2012 the U.S. Department of Agriculture started a zero tolerance policy against six non-O157 STEC groups (the ‘big six’) that cause over 70% of the total non-O157 illnesses. The new regulation requires a 2 step quantitative PCR (qPCR) that makes the screening process more expensive and labor intense [3]. We are creating a biological microchip that will run parallel amplification of target DNA reducing time and cost of detection assays.
منابع مشابه
Development of a multiplex loop-mediated isothermal amplification assay to detect shiga toxin-producing Escherichia coli in cattle
A multiplex loop-mediated isothermal amplification (mLAMP) assay was developed for simultaneous detection of the stx1 and stx2 genes and applied for detection of shiga toxin-producing Escherichia coli (STEC) in cattle farm samples. Two target genes were distinguished based on Tm values of 85.03 ± 0.54°C for stx1 and 87.47 ± 0.35°C for stx2. The mLAMP assay was specific (100% inclusivity and exc...
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